US2284267A - Stabilization of nonviscous cracked petroleum distillates - Google Patents

Stabilization of nonviscous cracked petroleum distillates Download PDF

Info

Publication number
US2284267A
US2284267A US351118A US35111840A US2284267A US 2284267 A US2284267 A US 2284267A US 351118 A US351118 A US 351118A US 35111840 A US35111840 A US 35111840A US 2284267 A US2284267 A US 2284267A
Authority
US
United States
Prior art keywords
vanadium
aldehyde
compounds
mol
primary amino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US351118A
Inventor
Frederick B Downing
Charles J Pedersen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US351118A priority Critical patent/US2284267A/en
Application granted granted Critical
Publication of US2284267A publication Critical patent/US2284267A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/228Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles
    • C10L1/2283Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles containing one or more carbon to nitrogen double bonds, e.g. guanidine, hydrazone, semi-carbazone, azomethine

Definitions

  • This invention relates to improvements in the stabilization of non-viscous cracked petroleum distillates and more particularly to the stabilization of cracked gasoline against the formation of gummy products and the loss of anti-knock value resulting from aging in the presence of air and traces of vanadium.
  • An object of the present invention is to retard the deterioration of non-viscous cracked petroleum distillates caused by the action of molecu lar oxygen and promotedby' the presence of vanadium and its compounds. Another object is pounds, will suppress the activity of the vanadium or its compounds.
  • a further object is to provide a method for rendering antioxidants more efiective for the preservation of non-viscous cracked petroleum distillates in the presence of vanadium and its compounds.
  • a still further object is to provide a class of organic compounds which, when added to cracked gasoline in the presence of an antioxidant and in the presence of vanadium or its compounds, increases the efliciency of the antioxidant.
  • Still further objects are to inhibit the formation of color, acids, gum, sludge and the like in mineral hydrocarbons containing or in contact with vanadium or its compounds.
  • Other objects are to provide new compositions of matter and to advance the art, Still other objects will appear hereinafter.
  • the polyamine may be an aliphatic amine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain and which amine may contain aromatic or other cyclic groups substituted on the chain.
  • the term aliphatic polyamine, as employed hereinafter and in the claims, will be understood to have the foregoing meaning.
  • the preferred polyamines are the alkylene polyamines, consisting of carbon, hydrogen and nitrogen, those in which at least two primary amino groups are directly attached to adjacent carbon atoms, and particularly the diamines.
  • adjacent atoms we mean atoms directly bondedtogether.
  • an "ortho-hydroxy substituted aldehyde” we mean one in which the hydroxy group and the aldehyde, or CHO, group are directly bonded to adjacent benzene ring carbon atoms.
  • aldehyde is preferably devoid of substituents other than hydrocarbon and hydroxy groups.
  • such aldehyde may contain, as substituents, alkoxy, aryloxy, halogen,heterocyclic,
  • polyamine may be likewise substituted but is preferably unsubstituted.
  • activator must be added for each gram atom of'
  • vanadium in the distillate Preferably, from vanadium in the distillate. about 1.5 to 100 mols of vanadium deactivator is used for each gram atom of vanadium in the distillate. From about 0.0002 to about 0.01% of vanadium deactivator, based on the cracked distillate, will generally be satisfactory in most cases where the vanadium or'vanadium compound is accidentally. present. Higher ratios of vanadium deactivator may be used, particularly when the cracked distillate is in contact with metallic vanadium in bulk which forms a reservoir of vanadium ions.
  • non-viscous cracked petroleum distillates we mean distillates obtained by the cracking of petroleum and which are in the boiling range of motor fuels and fuel oils and intend to include furnace oils and Diesel fuels, as well as cracked gasoline.
  • our compounds are resistant-to the action of molecular oxygen andsolutions of our compounds may be kept in the presence of air for years without any apparent change.- They are thermally stable at temperatures appreciably above their melting points, but are destroyed by strong mineral acids or hot dilute mineral acids. They are generally colored yellow of varying shade and intensity, and 0 tiilates treated in accordance with our invention will contain or be in contact with vanadium, they may also contain other contaminants and additives such as copper and iron and their derivatives, tetraethyl lead, dyes, colorv stabilizers, gum solvents and overhead lubricants.
  • deactivators may be used, as well I as the condensation products oi? a given polyamine with a mixture of aldehydes or a given aldehyde with a mixture of polyamines.
  • the compounds, obtained by condensing each of the following 'aldehydes with each of the iollowingpolyamines, are vanadium deactivators:
  • the method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distillate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an allphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • the method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distillate, normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an aldehydeaminecondensation product of the Schifls base type identical with Iii) that obtained by condensing 1 mol of an allphatic polyamlne containing exactly two primary amino-groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehydereacts for each primary amino group of the amine.
  • the method of inhibiting the catalytic deterioration of a, non-viscous cracked petroleum distillate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a-sinall proportion of an aldehyde-amine condensation product of the Schiff's base type identical with that obtained by condensing 1 mol of an alkyl diamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • the method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distfllate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an antioxidant normally effective to prevent deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the Schifi"s base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • the method of inhibiting the catalytic deterioration of cracked gasoline normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the cracked gasoline a small proportion of an antioxidant normally efiective to prevent deterioration of the cracked gasoline in the absence of vanadium and its compounds but which is less efiective in the. presence of v vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the SchiiFs base type identical with that obtained by condensing 1 mol of an aliphatic polyamine conta ning at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed-by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an aliphatic poly- I amine containing at least two. primary amino having-incorporated therein a small proportion of an aldehye-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing only two primary amino groupsfdirectly. attached to difierent carbon.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an aliphatic.diamine in which the two amino groups are primary amino groups directly attached to difierent adjacent carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde which, except for the OH and CH groups, consists of carbon and hydrogen, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an alkylene diamine in which the two amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion.
  • a non-viscous cracked petroleum distillate normally subject to deterioration causedby oxygen and catalyzed by vanadium or its compounds having incorporated therein asmall proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an alkylenediamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an orthohydroxy substituted aromatic aldehyde of the benzene series, so that not more than one mol of aldehyde reacts for each primary 5 amino group of the amine.
  • an aldehyde-amine of an antioxidant normally effective to materially retard deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an'aldehyde amine condensation product of the Schiffs basetype identical with that obtained by condensing 1 mol of an aliphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or. its compounds havingincorporated therein a small proportion of an antioxidant normally effective to materially retard deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing only two primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
  • a cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing'at least two primary amino groups directly attached to different carbon atoms of the some open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more'than one mol of aldehyde reacts for each primary amino group of the amine. 17.
  • a cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated condensation product of the Schiifs base type identical with that obtained by condensing 1 mol of an aliphatic poiyamine containing only two primary amino groups directly attached to difierent carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the e.
  • a cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an allrylene diamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde which, except for the hydroxy group and the -CH0 group consists of carbon and hydrogen, so that not more than one mol or aldehyde reacts ior each primary amino group oi the amine,
  • a cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of disalicylal 1,2- propylenediamine.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen andcatalyzed by vanadium or its compounds having incorporated therein a small proportion of di-(2-hydroxy-3-methoxybenzal) propylenediamlne.
  • a non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of disalicylal triethylenetetramlne.

Description

Patented May 26, 1942 UNE'E'E STATES greater FHQE STABILIZATION F NONVISCOUS CRACKED PETROLEUM DISTILLATES corporation of Delaware No Drawing. Application August 3, 1940, Serial 21 Claims.
This invention relates to improvements in the stabilization of non-viscous cracked petroleum distillates and more particularly to the stabilization of cracked gasoline against the formation of gummy products and the loss of anti-knock value resulting from aging in the presence of air and traces of vanadium.
It is well known that the non-viscous cracked petroleum distillates, such as fuel oils and cracked gasoline, tend to deteriorate in thepresence of air with the formation of gummy. substances. The aging of cracked gasoline in the presence of air results in the formation of gum and the development of color. When the gum content exceeds a certain value (approximately mg./100 c. c. by the A. S. T. M. air jet method) the gasoline is considered unfit for use in gasoline motors. The deterioration of gasoline caused by the action of atmospheric oxygen can be retarded by the addition of compounds called gasoline antioxidants" or gum inhibitors." Inhibitors in cracked gasoline Eglofi, Morrell, Lowry, Jr. and Dryer, J. I. E. C. 24 1375 (1932); Inhibitors in cracked gasoline Lowry, Jr., Eglofi', Morrell and Dryer, J. I. E. C. 25 804 (1933); Gum formation in gasoline Rogers and Voorhees, J. I. E. C. 25 520 (1933).
Copper and its compounds accelerate the rate of oxidation of cracked gasoline and most of the commonly used organic antioxidants. Hence copper and antioxidants are antagonistic in action, and the normal inhibiting effect of the latter is greatly reduced in the presence of the former] Compounds capable of efiectively suppressing the catalytic activity of copper-and its compounds in gasoline and methods of utilizing them are described in U. S. Patents 2,181,121 and It has also been found that vanadium and its compounds increase the rate of deterioration of the non-viscous cracked petroleum distillates, even when they are stabilized with antioxidants. Vanadium occurs naturally in some crude petroleums, particularly in the crudes found in Venezuela and Iran, and see The Science of Petro-- leum Thomas. vol. II, p. 1053 (1937).
An object of the present invention is to retard the deterioration of non-viscous cracked petroleum distillates caused by the action of molecu lar oxygen and promotedby' the presence of vanadium and its compounds. Another object is pounds, will suppress the activity of the vanadium or its compounds. A further object is to provide a method for rendering antioxidants more efiective for the preservation of non-viscous cracked petroleum distillates in the presence of vanadium and its compounds. A still further object is to provide a class of organic compounds which, when added to cracked gasoline in the presence of an antioxidant and in the presence of vanadium or its compounds, increases the efliciency of the antioxidant. Still further objects are to inhibit the formation of color, acids, gum, sludge and the like in mineral hydrocarbons containing or in contact with vanadium or its compounds. Other objects are to provide new compositions of matter and to advance the art, Still other objects will appear hereinafter.
The above and other objects may be accomplished in accordance with our invention which comprises incorporating, in non-viscous cracked petroleum distillates, which are subject to deterioration normally caused by oxygen in the presence of vanadium and its compounds, aldehyde-amine condensation products of the type of arylidene amines or Schiffs bases, identical with those obtained by condensing one mol of an aliphatic polyamine, containing at least two primary amino groups capable of reacting with aromatic aldehydes to form'arylidene amines, with at least two mols of an ortho-hydroxy substituted aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
The polyamine may be an aliphatic amine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain and which amine may contain aromatic or other cyclic groups substituted on the chain. The term aliphatic polyamine, as employed hereinafter and in the claims, will be understood to have the foregoing meaning. The preferred polyamines are the alkylene polyamines, consisting of carbon, hydrogen and nitrogen, those in which at least two primary amino groups are directly attached to adjacent carbon atoms, and particularly the diamines.
By adjacent atoms," we mean atoms directly bondedtogether.
By an "ortho-hydroxy substituted aldehyde." we mean one in which the hydroxy group and the aldehyde, or CHO, group are directly bonded to adjacent benzene ring carbon atoms. The
aldehyde is preferably devoid of substituents other than hydrocarbon and hydroxy groups. However, such aldehyde may contain, as substituents, alkoxy, aryloxy, halogen,heterocyclic,
amino, ccyano, carboxyl and sulfonicgroups, as
-well as hydroxy, alkyl and aryl radicals. The
minutes. This effect was overcome by the addition of 0.005% disaiicylal-ethylenediamine.
polyamine may be likewise substituted but is preferably unsubstituted.
activator must be added for each gram atom of' Preferably, from vanadium in the distillate. about 1.5 to 100 mols of vanadium deactivator is used for each gram atom of vanadium in the distillate. From about 0.0002 to about 0.01% of vanadium deactivator, based on the cracked distillate, will generally be satisfactory in most cases where the vanadium or'vanadium compound is accidentally. present. Higher ratios of vanadium deactivator may be used, particularly when the cracked distillate is in contact with metallic vanadium in bulk which forms a reservoir of vanadium ions.
By "non-viscous cracked petroleum distillates, we mean distillates obtained by the cracking of petroleum and which are in the boiling range of motor fuels and fuel oils and intend to include furnace oils and Diesel fuels, as well as cracked gasoline.
In order to illustrate our invention, the results ot'some of the experimental tests are given:
These results were obtained by means of the induction period method developed by Voorhees and Eisinger (S. A. E. J. 24, 584 (1929)), and consists in shaking l00.c. c. of gasoline at 100 C. inn 1 liter Pyrex flask containing pure oxygen. The internal pressure is observed every ten minutes by means of a manometer attached. to the system. The elapsed time, from the start of the test until the gasoline begins to absorb oxygen at the rate of c. c. per 10 minutes as shown by the fall in internal pressure, is taken as the induction period. It has been found that the induction period, obtained by this method, although greatly shortened, is a fairly accurate measure of the relative stability of gasoline under normal storage conditions.
TABLE I The eflect of dissolved vanadium [Gasoline inhibited with 0.002% by weight of p-benzylaminophenol] v I Induction period in minutes No Cone. deactivators, weight percent 1 No added V 1 P. P. M. V
1 None 330 180 2 0.005 460 800 It will be observed that the addition oi. 1 part per million of dissolved vanadium decreased the induction period of. the gasoline containing 0.002% p-benzylaminophenol from 330 to 180 a suitable solvent such as water, methanol or Vanadium was The vanadium deactivators oi the class of the present invention are well known compounds and the methods of preparing the same are described in the literature. They are readily prepared by reacting the required molal proportions of aldehyde and polyamine with or without the use of ethanol. The reactions are exothermic and water is formed. Nearly theoretical yields of the compounds" are obtained. The chemical equation for the formation of di (2-hydroxy benzal)- ethylenediamine may be represented as follows:
OH H0 The solubility of our compounds in the organic substances is dependent upon their constitution. For example, with a given polyamine, a ringalkylated' Z-hydroxybenzaldehyde yields a more soluble product than 2-hydroxybenzaidehyde. With a given'aldehyde, hexamethylenediamine forms a more soluble deactivator than ethylene diamine. Our com'pounds'are only slightly soluble in water except when they are solubilized with certain groups such as the suifonic acid and carboxyl groups, or when the hydrogen atoms of the hydroxyl groups are replaced by suitable cations such as sodium or potassium ions.
Unlike antioxidants, our compounds are resistant-to the action of molecular oxygen andsolutions of our compounds may be kept in the presence of air for years without any apparent change.- They are thermally stable at temperatures appreciably above their melting points, but are destroyed by strong mineral acids or hot dilute mineral acids. They are generally colored yellow of varying shade and intensity, and 0 tiilates treated in accordance with our invention will contain or be in contact with vanadium, they may also contain other contaminants and additives such as copper and iron and their derivatives, tetraethyl lead, dyes, colorv stabilizers, gum solvents and overhead lubricants.
Mixtures of deactivators may be used, as well I as the condensation products oi? a given polyamine with a mixture of aldehydes or a given aldehyde with a mixture of polyamines. Besides many others, the compounds, obtained by condensing each of the following 'aldehydes with each of the iollowingpolyamines, are vanadium deactivators:
Aldehydes: Polyarnines:
Z-bydroxybenzaldehyde ethylcnodiamine 2-hyd roxy-S-chlorobenzaldehyde 1,2-propylenediami Z-hyoroxy-G-methylbenzaldeh de z-hydroxy-d-methoisrbenzalde yde z-hydroxynaphthal ehyde-l 2,3-butylenodiami 3,4dialninohexan trimethyienedia i triethylenetetra i ffaasaaer Di (2 hydroiwbenzal) 1,2 propylenediamine.
Aldehydes: lolynminvs:
2-hydroxybenmldchyde mothylvnmlinmilu- 2-hydroxy-5-chlorobcnzaldch ydc ethylonmlimninc 2-hydroxy-3154iibromobenmldchydc Z-hydroxy-ti-mcthylhcnmldchyde Z-hydroxy-S-mcthoxybcnznldchydc 2:4-dihydroxyhcnzaldehyrlc 2:6-dihydroxybonzaldehyde Z-hydroxy-Ztcyanohcnmldehydo 2-hydroxy-Zi-carhoxybcnmldchy l 2-hydroxybenzaldehylc.'i-sulionic ucill 2-hydmxynaphthaldohydc-I l-hydroxynaphthaldchydc-Z anthrol-2-aldchyde-l 2-21ydroxyHumane-aldehyde! 4-hydrox ydiphenyl-alriehydc-R 3-hydroxyphcnmithrcnemldvh ade-4 It will be apparent that by this invention. we have made it possible to enect the stabilization of non-viscous cracked petroleum distlllates, Particularly cracked gasoline. when contaminated with vanadium and its derivatives. It is generally unfeasible to remove the vanadium by other methods and it is usually not economical-Ito counteract the catalytic action of vanadium by means of an antioxidant alone. We believe that the vanadium deactivators form very stable complex chemical compounds with the vanadium, which complex chemical compounds possess little or no pro-oxidant catalytic properties.
While we have disclosed the preferred embodiments of our invention and the preferred modes of carrying the same into effect, it will be readily apparent to those skilled in the art that such disclosures are given for illustrative purposes and that many variations and modifications may be made therein without departing from the spirit of our'invention. Accordingly, we propose to claim our invention broadly as in the appended claims and not be limited by the specific embodiments particularly disclosed.
We claim:
l. The method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distillate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an allphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
2. The method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distillate, normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an aldehydeaminecondensation product of the Schifls base type identical with Iii) that obtained by condensing 1 mol of an allphatic polyamlne containing exactly two primary amino-groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehydereacts for each primary amino group of the amine.
3. The method of'inhibiting the catalytic deterioration .0! a non-viscous cracked petroleum distillate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an aldehyde-amine condensation product of the Schifi's base type identical with that obtained by condensing 1 mol of an aliphaticdiamine in which the amino groups are primary amino groups directly attached to adjacent carbon atoms of the same open chain with -2 mols of an ortho-hydroxy substitt ed aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group ofthe amine.
4. The method of inhibiting the catalytic deterioration of a, non-viscous cracked petroleum distillate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a-sinall proportion of an aldehyde-amine condensation product of the Schiff's base type identical with that obtained by condensing 1 mol of an alkyl diamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
5. The method of inhibiting the catalytic deterioration of a non-viscous cracked petroleum distfllate normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the said distillate a small proportion of an antioxidant normally effective to prevent deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the Schifi"s base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
6. The method of inhibiting the catalytic deterioration of cracked gasoline normally caused by vanadium and its compounds in the presence of oxygen which comprises incorporating in the cracked gasoline a small proportion of an antioxidant normally efiective to prevent deterioration of the cracked gasoline in the absence of vanadium and its compounds but which is less efiective in the. presence of v vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the SchiiFs base type identical with that obtained by condensing 1 mol of an aliphatic polyamine conta ning at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so
that not more than one mol of aldehyde reacts for each primary amino group of the amine.
'7. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed-by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an aliphatic poly- I amine containing at least two. primary amino having-incorporated therein a small proportion of an aldehye-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing only two primary amino groupsfdirectly. attached to difierent carbon.
atomsof' the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that-not more than one mol of aldehyde reacts for each primary amino group of the amine. "9. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an aliphatic.diamine in which the two amino groups are primary amino groups directly attached to difierent adjacent carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde which, except for the OH and CH groups, consists of carbon and hydrogen, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
I 10. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an alkylene diamine in which the two amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
11. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion.
of an aldehyde-amine condensation product of the Schiifs base type identical with that ob tained by condensing 1 mol of an alkylene diamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an 'ortho-hydroxy substituted aromatic aldehyde which, except for the hydroxy group and the ---CH0 group consists or carbon and hydro-' mol of aldehyde gen, so that not more than one reacts for each primary amino group of the amine.
12. A non-viscous cracked petroleum distillate normally subject to deterioration causedby oxygen and catalyzed by vanadium or its compounds having incorporated therein asmall proportion of an aldehyde-amine condensation product of the Schiffs base type identical with that obtained by condensing 1 mol of an alkylenediamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an orthohydroxy substituted aromatic aldehyde of the benzene series, so that not more than one mol of aldehyde reacts for each primary 5 amino group of the amine.
' therein a small proportion of an aldehyde-amine of an antioxidant normally effective to materially retard deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an'aldehyde amine condensation product of the Schiffs basetype identical with that obtained by condensing 1 mol of an aliphatic polyamine containing at least two primary amino groups directly attached to different carbon atoms of the same open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
15. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or. its compounds havingincorporated therein a small proportion of an antioxidant normally effective to materially retard deterioration of the said distillate in the absence of vanadium and its compounds but which is less effective in the presence of vanadium and its compounds and a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing only two primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the amine.
16. A cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an aliphatic polyamine containing'at least two primary amino groups directly attached to different carbon atoms of the some open chain with at least 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more'than one mol of aldehyde reacts for each primary amino group of the amine. 17. A cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated condensation product of the Schiifs base type identical with that obtained by condensing 1 mol of an aliphatic poiyamine containing only two primary amino groups directly attached to difierent carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde, so that not more than one mol of aldehyde reacts for each primary amino group of the e.
18. A cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of an aldehyde-amine condensation product of the Schifis base type identical with that obtained by condensing 1 mol of an allrylene diamine in which the amino groups are primary amino groups directly attached to different carbon atoms of the same open chain with 2 mols of an ortho-hydroxy substituted aromatic aldehyde which, except for the hydroxy group and the -CH0 group consists of carbon and hydrogen, so that not more than one mol or aldehyde reacts ior each primary amino group oi the amine,
19. A cracked gasoline normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of disalicylal 1,2- propylenediamine.
20. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen andcatalyzed by vanadium or its compounds having incorporated therein a small proportion of di-(2-hydroxy-3-methoxybenzal) propylenediamlne.
21. A non-viscous cracked petroleum distillate normally subject to deterioration caused by oxygen and catalyzed by vanadium or its compounds having incorporated therein a small proportion of disalicylal triethylenetetramlne.
FREDERICK B. DOWNING. CHARLES J. PEDERSEN.
US351118A 1940-08-03 1940-08-03 Stabilization of nonviscous cracked petroleum distillates Expired - Lifetime US2284267A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US351118A US2284267A (en) 1940-08-03 1940-08-03 Stabilization of nonviscous cracked petroleum distillates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US351118A US2284267A (en) 1940-08-03 1940-08-03 Stabilization of nonviscous cracked petroleum distillates

Publications (1)

Publication Number Publication Date
US2284267A true US2284267A (en) 1942-05-26

Family

ID=23379645

Family Applications (1)

Application Number Title Priority Date Filing Date
US351118A Expired - Lifetime US2284267A (en) 1940-08-03 1940-08-03 Stabilization of nonviscous cracked petroleum distillates

Country Status (1)

Country Link
US (1) US2284267A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2533205A (en) * 1947-10-27 1950-12-12 Universal Oil Prod Co Metal deactivators
US3043783A (en) * 1960-03-31 1962-07-10 Universal Oil Prod Co Metal deactivator composition of low freezing properties
US3048480A (en) * 1959-06-09 1962-08-07 Gulf Research Development Co Aviation turbine fuels
US3053645A (en) * 1958-12-22 1962-09-11 Sinclair Research Inc Fuel composition
US3304162A (en) * 1963-06-25 1967-02-14 Du Pont Stabilized fuel oil compositions
US3328285A (en) * 1965-01-06 1967-06-27 Petrolite Corp Hydrocarbon inhibitor for use in heat exchangers of oil refinery equipment
US3336124A (en) * 1964-08-25 1967-08-15 Du Pont Stabilized distillate fuel oils and additive compositions therefor
US3490882A (en) * 1966-08-11 1970-01-20 Du Pont Stabilized distillate fuel oils and additive compositions therefor
US4003719A (en) * 1975-02-05 1977-01-18 Texaco Inc. Schiff bases as biocides in petroleum products
US4737159A (en) * 1984-06-29 1988-04-12 E. I. Du Pont De Nemours And Company Corrosion inhibitor for liquid fuels

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2533205A (en) * 1947-10-27 1950-12-12 Universal Oil Prod Co Metal deactivators
US3053645A (en) * 1958-12-22 1962-09-11 Sinclair Research Inc Fuel composition
US3048480A (en) * 1959-06-09 1962-08-07 Gulf Research Development Co Aviation turbine fuels
US3043783A (en) * 1960-03-31 1962-07-10 Universal Oil Prod Co Metal deactivator composition of low freezing properties
US3304162A (en) * 1963-06-25 1967-02-14 Du Pont Stabilized fuel oil compositions
US3336124A (en) * 1964-08-25 1967-08-15 Du Pont Stabilized distillate fuel oils and additive compositions therefor
US3328285A (en) * 1965-01-06 1967-06-27 Petrolite Corp Hydrocarbon inhibitor for use in heat exchangers of oil refinery equipment
US3490882A (en) * 1966-08-11 1970-01-20 Du Pont Stabilized distillate fuel oils and additive compositions therefor
US4003719A (en) * 1975-02-05 1977-01-18 Texaco Inc. Schiff bases as biocides in petroleum products
US4737159A (en) * 1984-06-29 1988-04-12 E. I. Du Pont De Nemours And Company Corrosion inhibitor for liquid fuels

Similar Documents

Publication Publication Date Title
US2181121A (en) Stabilization of organic substances
EP2113020B1 (en) Fuel composition and its use
US2284267A (en) Stabilization of nonviscous cracked petroleum distillates
US2181122A (en) Stabilization of organic substances
US2647824A (en) Stabilized compositions containing hydrogenated quinolines with oxidation inhibitors
US3490882A (en) Stabilized distillate fuel oils and additive compositions therefor
US2420122A (en) Suppression of metal catalysts
US3092475A (en) Fuel composition
US4743273A (en) Fuel composition and method for control of engine octane requirements
US4844717A (en) Fuel composition and method for control of engine octane requirements
US3809719A (en) Organic compositions containing amino-guanidine antioxidants
US2305676A (en) Treatment of gasoline
US2683081A (en) Stabilized organic compositions
US2696427A (en) Stabilized fuel oil compositions
US2641539A (en) Preventing discoloration of fuel oil
US4773916A (en) Fuel composition and method for control of octane requirement increase
AU2009333162A1 (en) Fuel composition and its use
US2530650A (en) Metal deactivator
US1971329A (en) Gum inhibitor
US2163640A (en) Inhibitor and motor fuel stabilized therewith
US2885274A (en) Motor fuel composition
US2917377A (en) Synergistic stabilizing compositions
US3084034A (en) Stable petroleum distillate fuels
US3190835A (en) Metal deactivators
US2813783A (en) Stabilization of organic compounds